A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060673



Internal ID20627713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27543622..27544592hg38UCSC Ensembl
chr1:27870133..27871103hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38971
hg19971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331048
Supporting Variants
Samples
Known GenesAHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060673
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer